Efficient analyte oxidation in an electrospray ion source using a porous flow-through electrode emitter

被引:39
作者
Van Berkel, GJ
Kertesz, V
Ford, MJ
Granger, MC
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Organ & Biol Mass Spect Grp, Oak Ridge, TN 37831 USA
[2] ESA, Chelmsford, MA USA
关键词
D O I
10.1016/j.jasms.2004.08.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This article describes the components, operation, and use of a porous flow-through electrode emitter in an electrospray ion source. This emitter electrode geometry provided enhanced mass transport to the electrode surface to exploit the inherent electrochemistry of the electrospray process for efficient analyte oxidation at flow rates up to 800 muL/min. An upstream current loop in the electrospray source circuit, formed by a grounded contact to solution upstream of the emitter electrode, was utilized to increase the magnitude of the total current at the emitter electrode to overcome current limits to efficient oxidation. The resistance in this upstream current loop was altered to control the Current and "dial-in" the extent of analyte oxidation, and thus, the abundance and nature of the oxidized analyte ions observed in the mass spectrum. The oxidation of reserpine to form a variety of products by Multiple electron transfer reactions and oxidation of the ferroceneboronate derivative of pinacol to form the ES active radical cation were used to study and to illustrate the performance of this new emitter electrode design. Flow injection, continuous infusion, and on-line HPLC experiments were performed. (C) 2004 American Society for Mass Spectrometry.
引用
收藏
页码:1755 / 1766
页数:12
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